MPS SOCIETY
KEDA are experts in their field who have been a great help in securing new funds for our organisation. We are so pleased KEDA were able to work on our statement to funders, explaining the current impact of COVID-19 on our community and income. They drafted the statement in record time. It has already proved an incredibly useful tool encouraging emergency funding from trusts and companies, including a grant of £90,000, which will enable us to weather the storm and continue to support our vulnerable community. Thank you!

Anna Featherstone, Head of Fundraising and Communications

The MPS Society support the rare disease community affected by Mucopolysaccharide diseases through research, information, support and advocacy.
We began working with the charity in 2019, as they needed help to develop larger grant applications. We began with research and a workshop to prioritise projects and services and share understanding of funder requirements. We now work with the MPS Society monthly, overseeing their trust fundraising programme.